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Dietary restriction transforms the mammalian protein persulfidome in a tissue-specific and cystathionine γ-lyase-dependent manner
Hydrogen sulfide (H(2)S) is a cytoprotective redox-active metabolite that signals through protein persulfidation (R-SS(n)H). Despite the known importance of persulfidation, tissue-specific persulfidome profiles and their associated functions are not well characterized, specifically under conditions...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979915/ https://www.ncbi.nlm.nih.gov/pubmed/33741971 http://dx.doi.org/10.1038/s41467-021-22001-w |
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author | Bithi, Nazmin Link, Christopher Henderson, Yoko O. Kim, Suzie Yang, Jie Li, Ling Wang, Rui Willard, Belinda Hine, Christopher |
author_facet | Bithi, Nazmin Link, Christopher Henderson, Yoko O. Kim, Suzie Yang, Jie Li, Ling Wang, Rui Willard, Belinda Hine, Christopher |
author_sort | Bithi, Nazmin |
collection | PubMed |
description | Hydrogen sulfide (H(2)S) is a cytoprotective redox-active metabolite that signals through protein persulfidation (R-SS(n)H). Despite the known importance of persulfidation, tissue-specific persulfidome profiles and their associated functions are not well characterized, specifically under conditions and interventions known to modulate H(2)S production. We hypothesize that dietary restriction (DR), which increases lifespan and can boost H(2)S production, expands tissue-specific persulfidomes. Here, we find protein persulfidation enriched in liver, kidney, muscle, and brain but decreased in heart of young and aged male mice under two forms of DR, with DR promoting persulfidation in numerous metabolic and aging-related pathways. Mice lacking cystathionine γ-lyase (CGL) have overall decreased tissue protein persulfidation numbers and fail to functionally augment persulfidomes in response to DR, predominantly in kidney, muscle, and brain. Here, we define tissue- and CGL-dependent persulfidomes and how diet transforms their makeup, underscoring the breadth for DR and H(2)S to impact biological processes and organismal health. |
format | Online Article Text |
id | pubmed-7979915 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79799152021-04-16 Dietary restriction transforms the mammalian protein persulfidome in a tissue-specific and cystathionine γ-lyase-dependent manner Bithi, Nazmin Link, Christopher Henderson, Yoko O. Kim, Suzie Yang, Jie Li, Ling Wang, Rui Willard, Belinda Hine, Christopher Nat Commun Article Hydrogen sulfide (H(2)S) is a cytoprotective redox-active metabolite that signals through protein persulfidation (R-SS(n)H). Despite the known importance of persulfidation, tissue-specific persulfidome profiles and their associated functions are not well characterized, specifically under conditions and interventions known to modulate H(2)S production. We hypothesize that dietary restriction (DR), which increases lifespan and can boost H(2)S production, expands tissue-specific persulfidomes. Here, we find protein persulfidation enriched in liver, kidney, muscle, and brain but decreased in heart of young and aged male mice under two forms of DR, with DR promoting persulfidation in numerous metabolic and aging-related pathways. Mice lacking cystathionine γ-lyase (CGL) have overall decreased tissue protein persulfidation numbers and fail to functionally augment persulfidomes in response to DR, predominantly in kidney, muscle, and brain. Here, we define tissue- and CGL-dependent persulfidomes and how diet transforms their makeup, underscoring the breadth for DR and H(2)S to impact biological processes and organismal health. Nature Publishing Group UK 2021-03-19 /pmc/articles/PMC7979915/ /pubmed/33741971 http://dx.doi.org/10.1038/s41467-021-22001-w Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bithi, Nazmin Link, Christopher Henderson, Yoko O. Kim, Suzie Yang, Jie Li, Ling Wang, Rui Willard, Belinda Hine, Christopher Dietary restriction transforms the mammalian protein persulfidome in a tissue-specific and cystathionine γ-lyase-dependent manner |
title | Dietary restriction transforms the mammalian protein persulfidome in a tissue-specific and cystathionine γ-lyase-dependent manner |
title_full | Dietary restriction transforms the mammalian protein persulfidome in a tissue-specific and cystathionine γ-lyase-dependent manner |
title_fullStr | Dietary restriction transforms the mammalian protein persulfidome in a tissue-specific and cystathionine γ-lyase-dependent manner |
title_full_unstemmed | Dietary restriction transforms the mammalian protein persulfidome in a tissue-specific and cystathionine γ-lyase-dependent manner |
title_short | Dietary restriction transforms the mammalian protein persulfidome in a tissue-specific and cystathionine γ-lyase-dependent manner |
title_sort | dietary restriction transforms the mammalian protein persulfidome in a tissue-specific and cystathionine γ-lyase-dependent manner |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979915/ https://www.ncbi.nlm.nih.gov/pubmed/33741971 http://dx.doi.org/10.1038/s41467-021-22001-w |
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